A quench column apparatus for separating methacrolein from methacrylic acid in a gas phase product from the partial oxidation of isobutene

ABSTRACT

A system and process for separating methacrolein (MA) from methacrylic acid (MAA) and acetic acid in the gas phase product from partial oxidation of isobutylene (IB) in two oxidation steps is disclosed. The process and system maximize recovery of all three components at minimum capital and energy cost, under conditions that minimize polymerization conditions and plugging by solids deposition in compressors, columns, etc.

RELATED APPLICATIONS

This application claims the benefit and priority as a divisionalapplication to U.S. patent application Ser. No. 11/706,800, filed 14Feb. 2007.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a method and system for the partialoxidation of isobutene having reduced methacrolein, methacrylic acid andacetic acid losses.

More particularly, the present invention relates to methods and systemsfor the partial oxidation of isobutene including the steps partiallyoxidizing an isobutene stream into a crude methacrylic acid containingstream in an oxidation subsystem. The crude methacrylic acid containingstream is instantaneously or near instantaneously quenched with asufficient amount of a recycle stream in a sump portion of a quenchcolumn of a quench/distillation subsystem, sending a first portion of abottoms product for methacrylic acid and acetic acid separation andpurification, recycling a second and major portion of the bottomsproduct as the recycle stream to quench the crude methacrylic acidcontaining stream, sending a portion of an overhead product from thequench/distillation subsystem to a methacrolein recovery orabsorber/stripper subsystem, recycling a major portion of the bottomstream from the stripper column to an upper portion of the absorbercolumn and forwarding a recovered methacrolein stream from the overheadof the stripper column to the oxidation subsystem.

2. Description of the Related Art

Many patents and publications disclose aspects of a process of partiallyoxidizing isobutene or an isobutene equivalent into methacrylic acid ina single step or multi-step oxidation process. Some of these patentsrelated directly to or extensively discuss quenching of the effluentfrom the partial oxidation of the isobutene or isobutene equivalentinput stream.

In U.S. Pat. No. 4,554,054 disclosed a process to recover acrylic acidor methacrylic acid by using a split quench process which allows acrylicacid or methacrylic acid to be recovered from the resulting aqueoussolutions by a combination of solvent extraction and azeotropicdehydration that minimizes the amount of solvent required.

In U.S. Pat. No. 4,618,709 disclosed a process for separation ofmethacrylic acid from a methacrylic acid-containing, gaseous reactionmixture obtained by subjecting methacrolein or a compound which canafford methacrolein under reaction conditions and molecular oxygen togas phase reaction in the presence of a catalyst for oxidation under thecoexistence of an inert gas for dilution which comprises (a) cooling thegaseous reaction mixture from a reactor wherein the gas phase reactionhas been effected to separate into condensable components includingmethacrylic acid, acetic acid and water vapor as a condensed liquor andnon-condensable components including methacrolein as a non-condensedgaseous mixture, (b) eliminating contaminating methacrolein from thecondensed liquor and (c) contacting the resulting condensed liquor withan organic solvent to extract methacrylic acid, followed by separationinto an organic solvent solution including methacrylic acid and anaqueous solution as waste water, characterized in that (1) the inert gasfor dilution is a non-condensable gas or its mixture with water vaporand (2) the aqueous solution ultimately separated is evaporated and theevolved vapor is subjected to catalytic combustion with molecularoxygen, whereby the amount of waste water to be discharged is muchsuppressed.

In U.S. Pat. No. 4,925,981 disclosed a method of isolating andrecovering methacrylic acid from a methacrylic acid-containing reactionproduct gas resulting from the vapor-phase catalytic oxidation ofisobutylene, tertiary butanol or isobutyraldehyde, which comprisesintroducing the reaction product gas comprising methacrylic acid andvarious by-products including high boiling substances at a hightemperature of 250° to 300° C. into a cooling zone, rapidly cooling thegas therein to a temperature of not more than 100° C. to condensemethacrylic acid and thus isolate methacrylic acid, while alsoconverting the high boiling substances to fumes, thereafter introducingthe cooled gas containing said fumes into a venturi scrubber, contactingit therein with an aqueous medium to remove said fumes, finallyintroducing the treated gas into a methacrylic acid-absorbing zone andabsorbing methacrylic acid by absorption into an aqueous medium.

In U.S. Pat. No. 4,956,493 disclosed a process for producing amethacrylic ester which comprises catalytically oxidizing isobutylene,tert-butanol, methacrolein or isobutyl aldehyde in a vapor phase;removing light-boiling substances form the resulting reaction product bydistillation or stripping; extracting methacrylic acid from theresulting methacrylic acid aqueous solution using a saturated chainaliphatic hydrocarbon having 6 to 9 carbon atoms as a solvent;recovering the solvent from the obtained solvent solution of methacrylicacid; esterifying the resulting methacrylic acid by the reaction of itwith a lower aliphatic alcohol or a lower alicyclic alcohol having 1 to12 carbon atoms using a porous strongly acidic cation exchange resin asa catalyst for esterfication; and then subjecting the thus obtainedesterification reaction product to a purification step.

In U.S. Pat. No. 4,987,252 disclosed in order to recover methacroleinand/or methacrylic acid by quenching a reaction product gas obtained bycatalytic oxidation of isobutylene or the like, the reaction product gasis charged into a quench column through a double-wall pipe and is thenbrought into contact with a condensate as a cooling medium. Depositionof terephthalic acid and the like inside the column is prevented bycontrolling the temperature of a bottom in the quench column and that ofan overhead gas of a quench column unit. An aromatic carboxylic acid,aromatic aldehyde, metal powder is added to an aqueous solution ofmethacrylic acid, which contains terephthalic acid and the like, so thatthe terephthalic acid and the like are caused to precipitate for theirremoval.

In U.S. Pat. No. 5,356,460 disclosed methacrolein is removed from agaseous mixture by absorption by means of an aqueous solution whichcontains from 60 to 90% by weight of methacrylic acid.

In U.S. Pat. No. 5,780,679 disclosed a process for the separation of(meth)acrylic acid from the reaction gas mixture formed in the catalyticgas phase oxidation by countercurrent absorption using a high-boilinginert hydrophobic organic liquid, in which the reaction gas mixture ispassed through an absorption column countercurrently to the descendinghigh-boiling inert hydrophobic organic liquid and (meth)acrylic acid issubsequently fractionally separated from the liquid effluent leaving theabsorption column and containing (meth)acrylic acid, wherein arectifying process is superimposed on the absorption process occurringnaturally in the absorption column by removing a quantity of energy fromthe absorption column which exceeds its natural energy loss resultingfrom contact with the ambient atmosphere.

In European Patent No. 0345083 B1 disclosed a process for recoveringmethacrolein which comprises: a reaction step (A) comprisingcatalytically oxidizing isobutylene, t-butanol, methacrolein, isobutylaldehyde or isobutyric acid or a mixture thereof with a gas containingmolecular oxygen in a vapor phase, a methacrylic acid condensation step(B) comprising contacting the reaction product gas obtained in step (A)with an aqueous phase containing methacrylic acid and acetic acid toobtain an aqueous solution of methacrylic acid, a methacrylic acidextraction step (C) comprising extracting methacrylic acid (page 24,lines 11 and 12) obtained in step (B) with an extraction solvent whichis a saturated hydrocarbon having 6 to 9 carbon atoms, and separatingthe extracted methacrylic acid to a solvent phase and an aqueous phasecontaining acetic acid, a methacrolein recovery step (D) comprisingcontacting the gas containing methacrolein and methacrylic aciddischarged from step (B) with an aqueous phase containing methacrylicacid and acetic acid to recover methacrolein and methacrylic acidcontained in said gas into said aqueous phase, a methacrolein desorptionstep (E) comprising contacting the aqueous phase containing methacrylicacid, acetic acid and methacrolein discharged from step (D) with a gascontaining molecular oxygen to desorb methacrolein, and a methacrylicacid recovery step (F) comprising contacting the gas containingmethacrylic acid and methacrolein desorbed from step (E) with an aqueousphase containing acetic acid to obtain a gas containing methacrolein, atthe same time recovering methacrylic acid into said aqueous phase, whichprocess comprises circulating the aqueous phase containing acetic aciddischarged from the methacrylic acid extraction step (C) in themethacrylic acid recovery step (F), circulating the aqueous phasecontaining methacrylic acid and acetic acid discharged from themethacrolein desorption step (E) in the methacrylic acid condensationstep (B) and/or the methacrolein recovery step (D) and circulating thegas containing methacrolein discharged from the methacrylic acidrecovery step (F) in the reaction step (A).

Although these patents and publications disclose many differentprocesses and equipment for achieving a rapid quenching and processingof the oxidation effluent, there is still a need in the art for a systemand a related process that rapidly quenches the oxidized effluent whileachieving reduced methacrolein, methacrylic acid and acetic acid losses.

SUMMARY OF THE INVENTION

The present invention provides a methacrylic acid production systemincluding an oxidation subsystem designed to oxidize isobutene into ahot oxidized stream including methacrolein (MA), methacrylic acid (MAA)and acetic acid (AA). The system also includes a quench/distillationsubsystem designed to rapidly (instantaneously or near instantaneously)quench the hot oxidized stream with a sufficient amount of a recyclestream to reduce the temperature of the hot oxidized stream to atemperature below about 75° C. and to separate the oxidized stream intoan MAA rich bottoms stream and an overhead stream, where the MAA richbottoms stream is separated into the recycle stream and an MAA productstream. The MAA rich bottoms stream will also include most of the AAproduced in the system, where the term most means that the MAA bottomsstream includes a least about 90% of the AA produced in the system. Incertain embodiments, the MAA rich bottoms stream includes at least about92.5% of the AA produced in the system. In other embodiments, the MAAbottoms stream includes at least about 95% of the AA produced in thesystem. The system also includes an absorber/stripper subsystem designedto remove unconverted MA for recycle to the oxidation subsystem and toproduce absorber stream and a second MAA rich stream, which in combinedwith the MAA product stream. The system can also include a stripper gassubsystem for incinerating absorber column overheads into a stripper gasstream used in a stripper column to strip unreacted MA for recycle tothe oxidation subsystem. The term near instantaneously or virtuallyinstantaneously means that the recycle stream is sufficient to reducethe temperature of the hot oxidized stream to a temperatures below about75° C. within a time span of less than or equal to 10 seconds. Incertain embodiments, the time span is less than to 5 seconds. In otherembodiments, the time span is less than to 3 seconds. In certainembodiments, the time span is between about 2 and 3 seconds.

The present invention also provides a quench column for quenching a hotoxidized effluent stream including a quench column having a sumpsection. In the sump section, the effluent stream is injected into thequench column above a liquid layer therein through a inlet. Just abovethe effluent inlet, a recycle stream is injected into the distillationvia a recycle inlet, which is generally a spray type apparatus. Theeffluent stream has a temperature at or above about 200° C. and therecycle stream has a temperature at or below about 100° C. The flowrates of the two streams are adjusted so that all or substantially allof the effluent stream is reduced from its high temperature to therecycle stream temperature very rapidly, instantaneously or nearinstantaneously. In certain embodiments, the effluent stream has atemperature at or above about 225° C. and the recycle stream has atemperature of about 70° C., and the flow rate are adjusted so that allor substantially all of the effluent stream is reduced from its hightemperature to the recycle stream temperature very rapidly,instantaneously or near instantaneously. In certain embodiments, theeffluent stream has a temperature at or above about 250° C. and therecycle stream has a temperature below about 70° C., and the flow rateare adjusted so that all or substantially all of the effluent stream isreduced from its high temperature to the recycle stream temperature veryrapidly, instantaneously or near instantaneously. Stated another way,the flow rate of the recycle stream and the flow rate of the effluentstream are adjusted so that the flow rate of the recycle stream issufficient greater than the flow rate of the effluent stream toinstantaneously or near instantaneously drop the temperature of theeffluent stream to the temperature of the recycle stream in a sump zoneof the quench column of the quench/distillation apparatus. Thequench/distillation also includes an overhead processing section thatproduces an MA rich stream and a liquid stream that is injected into atop inlet of the quench column of the quench/distillation apparatus toimprove MA, MAA and AA separation efficiency in the quench/distillationapparatus.

The present invention also provides an absorber/stripper apparatushaving improved MA recovery for further partial oxidation. Theabsorber/stripper apparatus includes an absorber column and a strippercolumn. The absorber column takes a vapor fraction stream from aquench/distillation system as an input stream into a bottom section ofthe absorber column, which is absorbed by two MAA rich stripper derivedstreams having different temperatures and introduced into an upper and atop inlet of the absorber column. The streams, absorber column size andconditions are adjusted so that the overhead stream is substantiallyfree of MA, MAA and AA and the bottoms stream includes substantially allof the MA, MAA and AA in the vapor fraction stream. The absorber bottomsare introduced into a top inlet of a stripper column where it is mixedwith an upcoming stripper gas introduced into a lower section of thestripper column. The stripper column also includes a reboiler, where aportion of a bottoms from the stripper column is heated and injectedinto a bottom inlet of the stripper column. The streams, stripper columnsize and column conditions are adjusted so that substantially all of theMA is taken as an overhead stream and the remainder of the bottoms fromthe stripper column make up the absorber streams, while another portionis combined with a MAA/AA rich stream for MAA/AA separation andpurification.

The present invention also provides a methacrylic acid production systemincluding an oxidation subsystem designed to oxidize isobutene into ahot oxidized stream including methacrolein (MA), methacrylic acid (MAA)and acetic acid (AA). The system also includes a quench and primarydistillation subsystem designed to rapidly quench the hot oxidizedstream with a sufficient amount of a recycle stream and to separate theoxidized stream into an MAA rich bottoms stream and an MA rich overheadstream. The MAA rich bottoms stream is divided into at least twostreams, the recycle stream and an MAA product stream, where the recyclestream is forwarded to a sump portion of the primary distillationsubsystem to quench the hot oxidized stream. The overhead stream isdivided into an overhead MAA rich recycle stream and a stream containingessentially all the unconverted MA, where the overhead recycle stream isforwarded to an upper portion of the primary distillation subsystem. Thesystem also includes a stripper and absorber subsystem designed toremove unconverted MA for recycle to the oxidation subsystem and toproduce a second MAA rich stream, which is combined with the MAA productstream. Optionally, a third portion of the MAA rich bottoms stream iscombined with the overhead recycle stream prior to forwarding the streamto the upper portion of the distillation subsystem.

The present invention provides a method for making methacrylic acid(MAA) from isobutene (IB) including the step of oxidizing IB in thepresence of oxygen and at least one oxidation catalyst to produce a hotoxidized stream comprising methacrolein (MA), MAA and acetic acid (AA).The hot oxidized stream is then feed into a sump portion a quench columnof a quench and distillation subsystem of an MA production system. Thehot oxidized stream is mixed with a large excess amount of a recyclebottoms stream sufficient to rapidly reduce a temperature of the hotoxidized stream to a temperature at or below about 70° C. The quenchcolumn also separates the oxidized stream into an MAA rich bottomsstream and an MAA lean overhead stream. The MAA rich bottoms stream isdivided into an MAA product stream and the recycle bottoms stream. TheMAA lean or MA rich overhead stream is divided into an MA recoverystream and an overhead recycle stream. The MA recovery stream isforwarded to a stripper/absorber subsystem, while the overhead recyclestream is forwarded to an upper portion of the quench column.Optionally, the overhead recycle stream is combined with a portion ofthe recycle bottoms stream prior to being forwarded to the upper portionof the quench column. The MA recovery stream is feed as a gaseous streaminto a bottom portion of an absorber column, which is absorbed into aliquid in the absorber. An absorber bottoms stream is forwarded to a topof a stripper column, while an absorber overhead stream is forwarded toan incinerator to form a stripper gas stream a portion of which isforwarded to a bottom portion of the stripper column. A stripperoverhead stream, which is rich in MA, is sent back to the oxidizationsubsystem for further oxidation to MA. A portion of a stripper bottomsstream is forwarded through a reboiler and recycled back to the bottomportion of the stripper column. Another portion of the stripper bottomsstream is forwarded to a surge tank to adjust stripper/absorber streamflows. A stripper bottoms stream from the surge tank is pressurized anda portion is combined with the MAA product stream and a second portionis cooled. A first portion of the cooled stripper bottom stream isforwarded to an upper port of the absorber column, while a secondportion of the cooled stripper bottom stream is forwarded to a top portof the absorber column.

The present invention provides a method for quenching a hot crudemethacrylic acid stream including the step of quenching the crudemethacrylic acid stream in a quench and primary distillation subsystemdesigned to rapidly quench the hot oxidized stream with a sufficientamount of a recycle stream and to separate the oxidized stream into anMAA rich bottoms stream and an MA rich overhead stream. The MAA richbottoms stream is divided into at least two streams, the recycle streamand an MAA product stream, where the recycle stream is forwarded to asump portion of the primary distillation subsystem to quench the hotoxidized stream. The overhead stream is divided into an overhead MAArich recycle stream and a stream containing essentially all the MA,where the overhead recycle stream is forwarded to an upper portion ofthe primary distillation subsystem. The system also includes a stripperand absorber subsystem designed to remove unconverted MA for recycle tothe oxidation subsystem and to produce a second MAA rich stream, whichis combined with the MAA product stream. Optionally, a third portion ofthe MAA rich bottoms stream is combined with the overhead recycle streamprior to forwarding the stream to the upper portion of the distillationsubsystem.

The present invention further provides a process of separation includingthe step of introducing a hot stream comprising methacrolein (MA),methacrylic acid (MAA) and acetic acid (AA) into a quench column at afeed port. After introduction, a bottoms stream is withdrawn from abottom port of the quench column. A first portion of the bottoms streamis introduced into the quench column above the feed port to quench thehot stream substantially instantaneously. A second portion of thebottoms stream is introduced to a top of the quench column, while athird portion of the bottoms stream is withdrawn as a MAA productstream. The process is controlled such that (1) a first mass ratio ofthe first portion of the bottoms stream to the hot stream is at least5:1, (2) a second mass ratio of the first portion of the bottoms streamto the second portion of the bottoms stream is at least 5:1, and (3) atemperature of the quench stream is at or below about 75° C.

The present invention further provides a quench column apparatusincluding a quench column. The quench column includes: (1) a feed portfor introducing a hot stream comprising methacrolein (MA), methacrylicacid (MAA) and acetic acid (AA) into the quench column, where the feedport is located above a liquid level in the quench column, (2) a bottomport for withdrawing a bottoms stream from the quench column, (3) a topport for withdrawing an overhead stream from the quench column, (4) aquench port for introducing a quench stream into the quench column,where the quench port is located above the feed port, and (5) an upperport for introducing a liquid stream comprising overhead condensiblesand a second portion of the bottoms stream to improve liquid-gasinteractions within the quench column. The apparatus also includes abottoms recycle system. The bottoms recycle stream includes: (1) a firstsplitter valve to divide the bottoms stream into a product stream and arecycle stream, and (2) a second splitter valve to divide the recyclestream into the quench stream and a top recycle stream. The apparatusalso includes a top recycle system. The top recycle system includes: (1)at least one separator to separate the overhead stream into a vaporstream and an overhead liquid stream, and (2) a mixing valve to combinethe liquid stream and the top recycle stream forming the liquid stream.The apparatus is operated so that a mass ratio of the first portion ofthe bottoms stream to the hot stream is at least 5:1, a mass ratio ofthe first portion of the bottoms stream to the second portion of thebottoms stream is at least 5:1, and a temperature of the quench streamis at or below about 75° C.

The present invention further provides a process for separating MAA andAA in a stripper/absorber system including the step of introducing astream comprising MA, MAA and AA to an absorber column through a lowerside port. Afterwards, a first absorbent stream is introduced into a topside port of the absorber column, and a second absorbent stream isintroduced into an upper side port of the absorber column. An absorberbottoms stream is withdrawn from a bottom port of the absorber column,and a waste overhead stream withdrawing from a top port of the absorbercolumn. The absorber bottoms stream is forwarded to a top input port ofa stripper column, while a stripper gas stream is introduced into alower side port of the stripper column. An overhead stream comprisingsubstantially all of the MA is withdrawn from a top output port of thestripper column, and a stripper bottoms stream is withdrawn from abottom port of the stripper column. A portion of the stripper bottomsstream is recycled through a reboiler to a bottom side port of thestripper column. A relatively small split stream is taken from theremaining liquid leaving the stripper bottom. The split stream iscombined with the aqueous stream taken from the quench condensaterecycle loop. The process is operated so that a mass ratio of the splitstream to the remaining liquid leaving the stripper bottom is governedby:

Y=C ₁ +C ₂ *X

where C₁ and C₂ are constants, Y is a ratio of mass flow in the splitstream to the remaining mass flow of the liquid from the bottom of thestripper column, and X is the remaining mass flow of the liquid from thebottom of the stripper column.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention can be better understood with reference to the followingdetailed description together with the appended illustrative drawings inwhich like elements are numbered the same:

FIG. 1 depicts a schematic diagram of an embodiment of the process andsystem of this invention;

FIG. 2A depicts an expanded schematic diagram of the oxidation subsystemof FIG. 1;

FIG. 2B depicts an expanded schematic diagram of the quench/distillationsubsystem of FIG. 1;

FIG. 2C depicts an expanded schematic diagram of the absorber/strippersubsystem of FIG. 1; and

FIG. 2D depicts an expanded schematic diagram of the stripper gassubsystem of FIG. 1.

DETAILED DESCRIPTION OF THE INVENTION

The inventors have found a system and process for separatingmethacrolein (MA) from methacrylic acid (MAA) and acetic acid (AA) in agas phase product from partial oxidation of isobutene (IB) can beperformed that maximizes the recovery of MA, MAA and AA at minimumcapital and energy cost, under conditions that minimize polymerizationand plugging by solids deposition in compressors, column, etc. Theinventor has also found that the system and process can be adjusted tomaximize process operation, improving MA recovery and conversion andreducing MAA losses.

This invention pertains to a system and process for separatingmethacrolein (MA) from methacrylic acid (MAA) and acetic acid in the gasphase product from partial oxidation of isobutylene (IB) in twooxidation steps. The objective is to maximize recovery of all three atminimum capital and energy cost, under conditions that minimizepolymerization conditions and plugging by solids deposition incompressors, columns, etc. Another objective is to maximize processoperability. These objectives are met by the following keycharacteristics of this system and process.

1. The initial quench of hot reaction gas from the second oxidation stepis accomplished in 2-3 seconds by recycled condensate in a sump sectionof a quench column amounting to a near or substantially instantaneousquench of the hot reactor gas due to an overwhelming flood of recycledcondensate in the sump section of the quench column. This rapid, near orsubstantially instantaneous, cooling minimizes by-product andpolymerization reactions that occur when the gas is more graduallycooled. The entering gas temperature from the second oxidation reactoris about 280° C. and the condensate temperature is less than 70° C., andin certain embodiments about 67° C. To accomplish this near orsubstantially instantaneous quenching of the hot gases from theoxidation subsystem, a ratio of mass of recycled condensate to amass ofentering hot gas is about 7:1, and ratio of mass of recycled condensateto a mass of condensibles in the hot gas is about 70:1, wherecondensibles refers to that part of the hot gases that will condenseunder the quench column conditions. These conditions take advantage ofthe minimum boiling azeotrope for water and MA, which preferentiallykeeps MA in the gas phase in relation to MAA and acetic acid. Less than0.1% of the unreacted MA from the second oxidation leaves in the liquidstream or bottoms stream, which is split from the recycled condensateand sent to MAA/acetic acid recovery. Thus, there is no need for costlyrecovery and recycle of unreacted MA back to the second oxidation stepfrom this stream.

2. The non-condensed reaction gases leave the sump section of the quenchcolumn into the bottom of the quench column. A portion of the recycledcondensate is cooled to about 55° C. using cooling water and enters thetop of the quench column. A ratio of a mass flow of the cooled recycledcondensate fed to top of the quench column to a mass flow of the recyclestream fed to the sump section of the quench is about 1:5. In certainembodiments, this mass ratio is about 1:5.5, and in other embodiments,the ratio is about 1:6. Because so much condensation takes place in thesump, there is reduced vapor and liquid traffic in the quench columnabove the sump. This allows a much smaller quench column diametercompared to having all of the recycled condensate fed to the top.

3. The vapor leaving the top of the quench column passes through aventuri scrubber to capture any fine particulates, formed from highboiling by-products in the oxidation reactors, into the liquid phasethat were not captured in the sump and quench column. Enough liquid fromthe re-circulating condensate is diverted to the scrubber to make thevolume ratio of gas to liquid entering the scrubber to be about 1000to 1. This greatly reduces fouling and plugging problems in thedownstream equipment.

4. The gas leaving the scrubber is separated from the liquid, compressedto about 10 psia and cooled to about 95° C. to partially condense it. Itpasses through another gas/liquid separator. The liquid is recycled backto the quench column and scrubber. These conditions of temperature andpressure are again controlled to take advantage of the minimum boilingazeotropic temperature of the MA/water binary. Thus, the gas leaving thequench area to the absorber/stripper system contains over 99.9% of theunreacted MA from the second oxidation reactor. It also contains about43% of the acetic acid and about 9% of the MAA. This stream isintentionally passed to the absorber/stripper system. By controlling therecirculation rates, temperature and pressure of condensate around thequench column and scrubber, MA solubility in the recirculating liquidbetween the absorber and stripper columns is increased, therebydecreasing the required size of these columns.

5. The gas leaving the quench area is compressed from about 5 psia toabout 49 psia before entering the absorber/stripper system. It isadvantageous to compress the gas at this point, because it furtherreduces the required size of the absorber column; it provides pressurefor ultimate recycle of inerts back to the first oxidation reactor andto the stripper column if needed; and it provides pressure for recycleof a MA stream back to the second oxidation reactor.

6. Recycled condensate used as the absorbent, enters the absorber columnat two places or port. At a top side port of the absorber, a firstportion of the absorbent feed stream is cooled to about 16° C. beforeentering the top port. At an upper side port located about 20% of theway down the absorber column, a second portion of the absorbent feedstream is cooled to about 21° C. before entering the upper port. A massflow ratio of the first portion of absorbent feed to the second portionof the absorbent stream is about 1:5. In certain embodiments, this massratio is about 1:5.5, and in other embodiments, this mass ratio is about1:57. This reduces the refrigeration load, while keeping product andby-product losses out the top of the absorber, as a percent of thosecomponents leaving the second oxidation reactor, to ˜nil for MA, to˜1.1% for acetic acid, and to ˜0.2% for MAA.

7. A bottoms stream from the absorber column is forwarded to a top inputport of a stripper column. Conditions in the stripper column arecontrolled so that the temperature at the bottom of the stripper columndoes not exceed about 118° C. to minimize polymerization and to ensurethat essentially zero MA leaves in a stripper column bottoms stream, andless than 0.1% of both acetic acid and methacrylic acid leave through atop output port of the stripper column. This can be achieved bycontrolling a pressure at a top portion of the stripper column to avalue of about 25 psia, and then varying a bottom liquid rate bycontrolling heat (e.g., steam) supplied to a reboiler. A relativelysmall split stream, containing acetic acid and MAA among othercomponents, is taken from the liquid leaving the stripper bottom. It hasbeen found that a split fraction assigned to this stream should becontrolled to vary in a direct linear manner to the bottom liquid flowrate in order to maintain stable column operation. The split stream iscombined with the aqueous stream taken from the quench condensaterecycle loop. The combined streams are sent for recovery of MAA andacetic acid products.

One method for operating the absorber/stripper subsystem is according tothe following relationship:

Y=C ₁ +C ₂ *X

where C₁ and C₂ are constants, Y is a ratio of mass flow in the splitstream to the mass flow of the remaining liquid from the bottom of thestripper column, and X is the remaining mass flow of the liquid from thebottom of the stripper column. These two variables, X and Y, cannot bevaried independently without causing the process to go unstable. Incertain embodiments, the constant C₁ has a value between about −0.035and about −0.055, while the constant C₂ has a value between about 0.05and about 0.07. In certain embodiments, the constant C₁ has a valuebetween about −0.04 and about −0.05, while the constant C₂ has a valuebetween about 0.055 and about 0.065. In other embodiments, C₁ has avalue of about −0.0431 and C₂ has a value of about 0.0596.

Overall recovery of both MAA and acetic acid is about 99.5% based on thegiven selectivities to these products in the oxidation reactions,assuming reaction to extinction of perfectly recycled MA. This isbelieved to be a superior recovery for both products compared to anyother processing method that has been disclosed for recovery of theseproducts from a two step oxidation of isobutylene or tertiary butylalcohol.

First System Embodiment

Referring now to FIG. 1, a system for producing methacrylic acid (MAA),generally 100, is shown to include an oxidation subsystem 102, astripper gas subsystem 130, a quench/distillation subsystem 140, and anabsorber/stripper subsystem 170.

Oxidation Subsystem

The oxidation subsystem 102 includes a first oxidation reactor 104having a first inlet 106 and a first outlet 108. The first inlet 106 isconnected to a first heat exchanger 110 via appropriate piping c10,which is in turn connected to a first mixing valve 112 via appropriatepiping c12. The first mixing valve 112 is connected to an isobutene (IB)feed 114, an oxidizing agent feed 116, and a steam feed 118 and arecycle inert diluents gas stream 119 via appropriate piping c14, c16and c18, respectively. The oxidizing agent feed 116 is actuallyconnected to an oxidizing agent dividing valve ov1 and the steam feed118 is actually connected to a steam mixing valve st1 by appropriatepiping not labeled. The inert diluents gas stream c110 is also connectedto the steam mixing valve st1.

The oxidation subsystem 102 also includes a second mixing valve 120connected to the first outlet 108 via appropriate piping c20, to theoxidizing agent dividing value ov1 via appropriate piping c22 and to atop port 180 of a stripper column 178 (as described herein) viaappropriate piping c24. The second mixing valve 120 is optionallyconnected to a second heat exchanger 122 via appropriate piping c26,which is in turn connect to a second oxidation reactor 124 at a secondinlet 126 via appropriate piping c28. The second oxidation reactor 124also includes a second outlet 128. The first and second reactors 104 and124 are generally multiple tube reactors filled with a catalyst orhaving one or more catalyst zones in the tubes and cooled by a heattransfer fluid circulated about the tubes. The first reactor 104generally includes a mixed metal oxide catalyst well known in the artfor oxidizing IB to a methacrolein. Non-limiting and exemplary examplesof suitable mixed metal oxide catalysts are disclosed in the followingU.S. Pat. Nos. 3,907,712, 3,928,462, 3,929,899, 3,933,751, 3,936,505,3,956,378, 4,012,449, 4,025,565, 4,035,418, 4,111,984, 4,170,570,4,171,454, 4,190,608, 4,224,193, 4,240,931, 4,250,339, 4,252,683,4,258,217, 4,261,858, 4,267,385, 4,267,386, 4,271,040, 4,272,408,4,292,203, 4,306,088, 4,306,090, 4,332,971, 4,339,355, 4,354,044,4,377,501, 4,380,664, 4,404,397, 4,413,147, 4,414,134, 4,424,141,4,446,328, 4,454,346, 4,489,170, 4,503,247, 4,511,671, 4,535,188,4,537,874, 4,547,588, 4,556,731, 4,558,029, 4,596,784, 4,732,884,4,778,930, 4,803,190, 4,816,603, 4,871,700, 4,916,103, 4,925,823,4,946,819, 4,954,650, 5,059,573, 5,072,052, 5,081,314, 5,082,819,5,094,990, 5,102,847, 5,132,269, 5,138,100, 5,144,090, 5,155,262,5,166,119, 5,183,936, 5,198,578, 5,221,653, 5,225,389, 5,245,083,5,250,485, 5,264,627, 5,276,178, 5,300,707, 5,349,092, 5,364,825,5,380,933, 5,491,258, 5,532,199, 5,602,280, 5,670,702, 5,684,188,5,728,894, 5,739,391, 5,817,865, 5,821,390, 5,856,259, 6,028,220,6,069,271, 6,171,571, and RE32,082, incorporated herein by reference.The second reactor 124 generally includes a heteropolyacid catalyst wellknown in the art for oxiding methacrolein to methacrylic acid.Non-limiting and exemplary examples of suitable heteropolyacid catalystsare disclosed in the following U.S. Pat. Nos. 3,840,595, 3,865,873,3,875,220, Re 29,901, 3,925,464, 3,954,856, 3,956,182, 3,959,384,3,965,163, 3,968,165, 3,968,166, 3,972,920, 3,978,003, 3,998,876,3,998,877, 4,000,088, 4,001,316, 4,017,423, 4,035,418, 4,042,533,4,042,625, 4,051,179, 4,052,450, 4,070,397, 4,101,448, 4,115,441,4,118,419, 4,124,634, 4,138,366, 4,165,296, 4,166,190, 4,169,070,4,172,051, 4,180,678, 4,212,767, 4,223,161, 4,255,466, 4,238,359,4,240,930, 4,250,054, 4,252,681, 4,252,682, 4,252,683, 4,259,211,4,261,858, 4,261,859, 4,261,860, 4,271,040, 4,272,408, 4,273,676,4,297,247, 4,301,030, 4,301,031, 4,305,843, 4,314,074, 4,319,042,4,320,227, 4,339,355, 4,341,900, 4,347,163, 4,356,316, 4,358,608,4,358,610, 4,364,844, 4,374,757, 4,377,501, 4,404,397, 4,409,128,4,415,752, 4,419,270, 4,424,141, 4,440,948, 4,443,555, 4,444,906,4,444,907, 4,454,346, 4,467,113, 4,469,810, 4,471,061, 4,471,062,4,489,170, 4,503,247, 4,521,618, 4,528,398, 4,530,916, 4,536,483,4,547,588, 4,558,028, 4,558,029, 4,564,607, 4,565,801, 4,595,778,4,621,155, 4,652,673, 4,720,575, 4,745,217, 4,757,038, 4,803,302,4,804,778, 4,814,305, 4,816,603, 4,891,347, 4,925,823, 4,925,980,4,954,650, 4,966,990, 4,968,838, 4,985,592, 5,093,521, 5,102,846,5,102,847, 5,104,844, 5,126,307, 5,153,162, 5,173,468, 5,198,579,5,206,431, 5,221,767, 5,239,115, 5,264,627, 5,420,091, 5,422,326,5,521,137, 5,550,095, 5,569,636, 5,618,974, 5,981,804, 5,990,348,6,043,184, 6,060,419, 6,169,202, 11/189,095, 11/189,116 and 11/189,126,incorporated herein by reference.

Quench/Distillation Subsystem

The second outlet 128 is connected to the quench/distillation subsystem140 at a feed inlet 141 of a quench column 142 via appropriate pipingc30. Typically, piping c30 would include jacketing along the length justoutside the wall of 142 to, and including, downward directed inlet 141.A small amount of essentially inert gas fed to the jacketed sidesurrounds the main product from the second reactor 124 as it enters thequench at the feed inlet 141 to minimize plugging of the feed inlet 141by solid deposition due to premature cooling. This inert gas could be aslip stream (not shown) from either c100, or low pressure steam from thefeed stream 118, for example. The feed inlet 141 is located in a sumpzone 143 of the quench column 142. The quench column 142 also includes arecycle inlet 144 located above the feed inlet 141, a bottoms outlet145, an overhead outlet 146, and an upper inlet 147. The feed inlet 141is generally located above a liquid level 148 in the sump zone 143.

The quench/distillation subsystem 140 also includes a first pump 149connected to the bottoms outlet 145 appropriate piping c32. The pump 149is in turn connect to a first dividing valve 150 via appropriate pipingc34 and to a third heat exchanger 151 via appropriate piping c36. Thethird heat exchanger 151 is connected to a second dividing valve 152 viaappropriate piping c38. The second dividing valve 152 is connected tothe recycle inlet 144 via appropriate piping c40 and to a third mixingvalve 153 via appropriate piping c42. The third mixing valve 153 isconnected to a third dividing valve 154 via appropriate piping c44. Thethird dividing valve 154 is connected to the upper inlet 147 viaappropriate piping c46.

The overhead outlet 146 is connected to a venturi valve 155 viaappropriate piping c48. The venturi valve 155 is also connected to thethird dividing valve 154 via appropriate piping c50 and to a firstseparator 156 via appropriate piping c52. The first separator 156includes a first vapor outlet 157 and a first liquid outlet 158. Thefirst vapor outlet 157 is connected to a first compressor 159 viaappropriate piping c54. The first compressor 159 is connected to afourth heat exchanger 160 via appropriate piping c56. The fourth heatexchanger 160 is connected to a second separator 161 via appropriatepiping c58. The fourth heat exchanger 160 can be a single heat exchangeror two heat exchangers in series, where the first is water cooled andthe second is cooled by refrigerant, thus not requiring the totalcooling load to be borne by expensive refrigeration. The secondseparator 161 includes a second vapor outlet 162 and a second liquidoutlet 163. The second vapor outlet 162 is connected to a secondcompressor 164 via appropriate piping c60.

The first liquid outlet 158 of the first separator 156 and the secondliquid outlet 163 of the second separator 161 are connected a fourthmixing valve 165 via appropriate piping c62 and c64, respectively. Thefourth mixing valve 165 is connected to a second pump 166 viaappropriate piping c66, which is in turn connected to the third mixingvalve 153 via appropriate piping c68, completing the quench/distillationsubsystem 140.

The quench/distillation subsystem 140 also includes a first surge tank167 connected to the first dividing valve 150 via appropriate pipingc70, which includes a first inlet 168 a, a second inlet 168 b and anoutlet 169.

Absorber/Stripper Subsystem

The absorber/stripper subsystem 170 includes an absorber column 171. Theabsorber column 171 includes a lower feed inlet 172 connected to thesecond compressor 164 via appropriate piping c72. The absorber 171includes a bottoms outlet 173, an overhead outlet 174, a top inlet 175and a upper inlet 176. The bottoms outlet 173 is connected to a thirdpump 177 via appropriate piping c74, which is in turn connected to astripper column 178 at a top feed inlet 179 via appropriate piping c76.The stripper column 178 also includes an overhead outlet 180, a recyclelower inlet 181, a stripper gas inlet 182 and a bottoms outlet 183. Thestripper column 178 also includes a fourth dividing valve 184 and are-boiler 185. The fourth dividing valve 184 is connected to the bottomsoutlet 183 and the re-boiler 185 via appropriate piping c78 and c80,respectively. The re-boiler 185 is also connected to the recycle lowerinlet 181 via appropriate piping c82. The fourth dividing valve 184 isalso connected to a second surge tank 186 via appropriate piping c84.The surge tank 186 is connected to a fourth pump 187 via appropriatepiping c86, which is in turn connect to a fifth dividing valve 188 viaappropriate piping c88. The fifth dividing valve 188 is connected to afifth heat exchanger 189 via appropriate piping c90, which is in turnconnected to a sixth dividing valve 190 via appropriate piping c92. Thesixth dividing valve 190 is connected to the upper inlet 176 viaappropriate piping c94 and to a sixth heat exchanger 191 via appropriatepiping c96. The sixth heat exchanger 191 is connected to the top inlet175 via appropriate piping c98. The fifth dividing value 188 is alsoconnected to the second inlet 168 b of the first surge tank viaappropriate piping c99.

The overhead outlet 180 of the stripper column 178 is connected tosecond mixing valve 120 via the piping c24. The overhead 174 of theabsorber column 171 is connected to the stripper gas subsystem 130 at afifth mixing valve 132 via appropriate piping c100. The stripper gasinlet 182 of the stripper column 178 is connected to a sixth dividingvalve 138 of the stripper gas subsystem 130 via appropriate piping c102.

Stripper Gas Subsystem

The stripper gas subsystem 130 includes the fifth mixing valve 132 whichis connected to an incinerator 134 via appropriate piping c104 andoptionally to piping c112 which forwards a stream to be incinerated tothe incinerator 134. The incinerator 134 is connected to a seventh heatexchanger 136 via appropriate piping c106, which is in turn connected tothe sixth dividing valve 138 via appropriate piping c108. The sixthdividing valve 138 is connected to the steam mixing valve st1 viaappropriate piping c110 and to the stripper gas inlet 182 of thestripper column 178 via the piping c102. The sixth dividing valve 138can also be connected to a piping c114 supporting a vent stream.

Operation of First System Embodiment

Referring now to FIGS. 2A-D, four expanded views of the system of theFIG. 1 are set forth, where the figures describe the operation of thefour components of the system of FIG. 1: the Oxidation Subsystem, FIG.2A, the Quench/distillation Subsystem, FIG. 2B, the Absorber/stripperSubsystem, FIG. 2C, and the Stripper Gas Subsystem, FIG. 2D.

Oxidation Subsystem

Referring now to FIG. 2A, the expanded view of the oxidation subsystem102 of FIG. 1 is shown and its operation described in terms of streams.The properties or parameters of each stream are associated with a point,where the properties and parameters of the stream include physicaland/or chemical parameters such as composition, pressure, temperature,state (liquid, mixed, vapor, etc.), or other relevant properties orparameters.

In the first mixing valve 112, an isobutene (IB) feed stream S10 havingparameters as at a point pt1 supplied by an isobutene supply 114, afirst oxidizing agent stream S12 having parameters as at a point pt3 anda mixed stream S14 having parameters as at a point pt5 are combined toform a first input stream S16 having parameters as at a point pt7. Themixed stream S14 having the parameters as at the point pt5 is derivedfrom a mixing valve st1, which combines a steam stream S18 and an inertdiluent recycle stream S20, having parameters as at points pt9 and pill,respectively. The stream S18 having the parameters as at the point pt9is supplied from the steam source 118; while the stream S20 having theparameters as at the point pt11 is supplied from the stripper gassubsystem 130. The oxidizing agent stream S12 having the parameters asat the point pt3 is derived from a dividing valve ov1, which issupported by an oxidizing agent feed stream S22 having parameters as ata point pt13, which comes from a oxidizing agent supply 116. Althoughthe IB feed stream S10 and oxidizing agent stream S12 are at amoderately low temperature of about 85° F., upon mixing with the steamstream S18 and the diluent stream S20, the combined stream issignificantly increased in temperature as set forth in Table I herein.

The first input stream S16 having the parameters as at the point pt7then passes through the first heat exchanger 110, where it is heated toform a heated first input stream S24 having parameters as at a pointpt15 in a first heat exchange step pt7-pt15. The heated first inputstream S24 having the parameter as at the point pt15 is then forwardedto the first oxidation reactor 104 where it is partially oxidized over amixed metal oxide catalyst (as described above) to from amethacrolein-containing stream S26 having parameters as at a point pt17.The methacrolein-containing stream S26 having the parameters as at thepoint pt17 is then forwarded to the second mixing valve 120, where it iscombined with a second oxidizing agent stream S28 having parameters asat a point pt19 and a methacrolein recycle stream S30 having parametersas at a point pt21 to form a second input stream S32 having parametersas at a point pt23. The methacrolein recycle stream S30 having theparameters as at the point pt21 is derived from the absorber/strippersubsystem 170 (as described below).

The second input stream S32 having the parameters as at the point pt23is then passed through the second heat exchanger 122, where it is heatedto form a heated second input stream S34 having parameters as at a pointpt25 in a second heat exchange step pt23-pt25. The heated second inputstream S34 having the parameters as at the point pt25 is then forwardedto the second oxidization reactor 124, where it is partially oxidizedover a heteropolyacid catalyst (as described above) to form a crudemethacrylic acid stream S36 having parameters as at a point pt27.

Quench/Distillation Subsystem Operational Description

Referring now to FIG. 2B, the expanded view of the oxidation subsystem140 of FIG. 1 is shown and its operation described in terms of streamsand streams parameters as described above. The crude methacrylic acidstream S36 having the parameters as at the point pt27 is feed into thequench column 142 of the quench/distillation subsystem 140 through theinlet 141 as described above. The crude methacrylic acid stream S36 israpidly cooled in the sump portion 143 of the quench column 142 by afirst recycle substream S38 having parameters as at a point pt29, whichis fed into the column 142 via the inlet 144, which is generally adownward directed spray apparatus. A flow rate of the first recyclestream S38 having the parameters as at the point pt29 is sufficientlygreater than a flow rate of the methacrylic acid stream S36 having theparameters as at the point pt27 to instantaneously or nearinstantaneously cool the methacrylic acid stream S36 from a temperatureabove 250° C. to a temperature below about 70° C. This rapid,instantaneous or near instantaneous, cooling reduces polymerization andincreases column efficiency. The term rapid and near instantaneouscooling means that the cooling takes place quickly enough to reduce thestream S36 from 250° C. to 70° C. in a matter of a few seconds, lessthan 30 seconds. In certain embodiments, the stream S36 is cooled inless than 15 seconds. In certain other embodiments, the stream S36 iscooled in less than 5 seconds.

At the bottoms outlet 145, an enriched methacrylic acid stream S40having parameters as at a point pt31 is withdrawn from the column 142.The enriched methacrylic acid stream S40 having the parameters as at thepoint pt31 is then pumped to a higher pressure in the first pump 149 toform a higher pressure methacrylic acid stream S42 having parameters asat a point pt33. The higher pressure stream S42 having the parameters asat the point pt33 is then forwarded to the first dividing valve 150,where the stream S42 is divided into a recycle stream S44 havingparameters as at a point pt35 and a methacrylic acid product stream S46having parameters as at a point pt37. The recycle stream S44 is passedthrough the third heat exchanger 151 to form a cooled recycle stream S48having parameters as at a point pt39. The cooled recycle stream S48 isthen divided into the first recycle substream S38 having the parametersas at the point pt29 and a second recycle substream S50 havingparameters as at a point pt41. The second recycle substream S50 isforwarded to the third mixing valve 153, where it is combined with astream S52 having parameters as at a point pt43 to form a combinedrecycle stream S54 having parameters as at a point pt45. The combinedrecycle stream S54 is forwarded to the third dividing valve 154, whereit is divided into a top recycle stream S56 having parameters as at apoint pt47 and a venturi carrier stream S58 having parameters as at apoint pt49.

The column 142 also produces an overhead stream S60 having parameters asat a point pt51, which exits the column 142 at the overhead outlet 146.The overhead stream S60 is forwarded to the venturi valve 155, where itis mixed with the venturi carrier stream S58. The venturi valve 155 isdesigned to remove fine particles from the overhead vapor stream S60 toproduce a two-phased overhead stream S62 with essentially all fineparticles contained in the liquid phase having parameters as at a pointpt53. The cleaned overhead stream S62 is forwarded to the firstseparator 156, where it is separated into a first vapor stream S64 withessentially no particulates having parameters as at a point pt55 and afirst liquid stream S66 having parameters as at a point pt57. The firstvapor stream S64 is forwarded to the first compressor 159 to form ahigher pressure stream S68 having parameters as at a point pt59. Thehigher pressure stream S68 is then passed through the fourth heatexchanger 160 (or two heat exchangers as described above) to form acooled partially condensed stream S70 having parameters as at a pointpt61, which is forwarded to the second separator 161. The partiallycondensed stream S70 is separated into a second vapor stream S72 havingparameters as at a point pt63 and a second liquid stream S74 havingparameters as at a point pt65.

The second liquid stream S74 is then forwarded to the fourth mixingvalve 165, where it is mixed with the stream S66 to form a combinedliquid stream S76 having parameters as at a point pt67. The stream S76is then pressurized in the second pump 166 to form the higher pressureliquid stream S52 having the parameters as at the point pt43. The secondvapor stream S72 having the parameters as at the point pt63 is thenpassed through the second compressor 164 to form a compressed stream S78having parameters as at a point pt69.

The product methacrylic acid stream S46 having the parameters as at thepoint pt37 is forwarded to the first inlet 168 a of the first surge tank167. A second methacrylic acid product stream S80 having parameters asat a point pt71 coming from the absorption/stripper subsystem 170 entersthe first surge tank 167 via the second inlet 168 b. A combinedmethacrylic acid product stream S82 having parameters as at a point pt73is then forwarded to methacrylic acid purification and utilizationsystems (not shown).

Absorber/Stripper Subsystem

Referring now to FIG. 2C, the expanded view of the absorber/strippersubsystem 170 of FIG. 1 is shown and its operation described in terms ofstreams and streams parameters as described above. The compressed streamS78 having the parameters as at the point pt69 is fed into theabsorption column 171 at the inlet 172. An absorber bottom stream S84having parameters as at a point pt75 is withdrawn from the bottomsoutlet 173 of the absorber column 171 and forwarded to the third pump177, where its pressure is increased to form a higher pressure bottomsstream S86 having parameters as at a point pt77. The stream S86 is thenfed into the top inlet 179 of the stripper column 178. In the strippercolumn 178, the down flowing absorber bottoms in the stream S86 aremixed with an upcoming gas flow from a stripper gas stream S88 havingparameters as at a point pt79 entering at the stripper gas inlet 182 anda reboiler stream S90 having parameters as at a point pt81 entering atthe reboiler inlet 181 under conditions so that the stripper column 178produces a bottoms stream S92 having parameters as at a point pt83 atthe bottoms outlet 183 enriched in methacrylic acid and the overheadstream S30 having the parameters as at the point pt21 at the overheadoutlet 180 enriched in methacrolein. The overhead stream S30 having theparameters as at the point pt21 is then mixed with the stream S28 havingthe parameters as at the point pt19 and the stream S26 having theparameter as at the point pt17 to form the stream S32 having theparameters as at the point p23, which after heating is oxidized in thesecond reactor 124 as described above.

The bottom stream S92 having the parameters as at the point pt83 isforwarded to the fourth dividing valve 184, where it is divided into afirst bottoms substream S94 having parameters as at a point pt85 and asecond bottoms substream S96 having parameters as at a point pt87. Thefirst substream S94 is forwarded to the reboiler 185, where it is heatedto form the stream S90 having the parameters as at the point pt81. Thesecond substream S96 having the parameters as at the point pt87 isforwarded to the second surge tank 186. A methacrylic acid rich streamS98 having parameters as at a point pt89 is withdrawn from the secondsurge tank 186 and forwarded to the fourth pump 187 to form a higherpressure methacrylic acid rich stream S100 having parameters as at apoint pt91. The stream S100 is then forwarded to the fifth dividingvalve 188 to form the methacrylic acid rich stream S80 having parametersas at a point pt71 and a higher pressure methacrylic acid recycle streamS102 having parameters as at a point pt93. The stream S102 is forwardedto the fifth heat exchanger 189 to form a cooled stream S104 havingparameters as at a point pt95. The cooled stream S104 is then dividedvia the sixth dividing valve 190 into an upper recycle stream S106having parameters as at a point pt97, which is fed into the absorbercolumn 171 at the upper inlet 176, and a cooled substream S108 havingparameters as at a point pt99. The cooled substream S108 is furtherheated to form a top recycle stream S110 having parameters as at a pointpt101, which is fed into the absorber column 171 at the top inlet 175.In the absorber column 171, the two methacrylic acid rich recycle streamS106 and S110 are used to absorb methacrolein in the stream S78 so thatit can be separated in the stripper column and recycled to the secondreactor, while an overhead stream S112 having parameters as at a pointpt103 withdrawn from the overhead outlet 174 of the absorber column issent to the incinerator 134 to form the stripper gas stream S88.

Stripper Gas Subsystem

Referring now to FIG. 2D, the expanded view of the stripper gassubsystem 130 of FIG. 1 is shown and its operation described in terms ofstreams and streams parameters as described above. The absorber overheadstream S112 having the parameters as at the point pt103, which is awaste lights stream, is fed into the mixing valve 132, where it can bemixed with an external waste stream S114 having parameters as at a pointpt105 to form an incinerator stream S116 having parameters as at a pointpt107. The incinerator stream S116, along with an oxygen stream (notshown) to supply oxygen as needed for combustion, is then passed throughthe incinerator 134 where it is burned to from a flue gas stream S118having parameters as at a point pt109. The flue gas stream S118 is thenforwarded to the sixth heat exchanger 136 to form a cooled flue gasstream S120 having parameters as at a point pt111. The cooled flue gasstream S120 is then forwarded to the sixth dividing valve 138, whichproduces the inert diluents recycle stream S20 having the parameters asat the point pt11, the stripper gas stream S88 having the parameters asat the point pt79 and a purge stream S122 having parameters as at apoint pt113.

The overall process can be further understood with reference to thefollowing stream/parameter tables. Table I tabulates certain criticalphysical/chemical properties of the stream associated with the oxidationsubsystem of the process flow diagrams of FIG. 2A-D. Table II tabulatescertain critical physical/chemical properties of the stream associatedwith the quench distillation subsystem of the process flow diagrams ofFIG. 2A-D. Table III tabulates certain critical physical/chemicalproperties of the stream associated with the absorber/stripper subsystemof the process flow diagrams of FIG. 2A-D. Table IV tabulates certaincritical physical/chemical properties of the stream associated with thestripper gas subsystem of the process flow diagrams of FIG. 2A-D.

TABLE I Stream Properties in Oxidation Subsystem Parameters S10 S12 S16S18 S20 S24 Temperature ° C. 29.44 29.44 183.1 162.39 259.78 225.00 (°F.) (85.00) (85.00) (361.60) (324.30) (499.60) (437.00) Pressure psi65.00 100.00 34.00 95.00 34.00 32.00 Vapor Frac 0.000 1.000 1.000 1.0001.000 1.000 Mole Flow lbmol/hr 504.23 606.21 8415.22 711.51 6593.278415.22 Mass Flow lb/hr 28291.20 19397.91 341420.85 12818.00 280913.74341420.85 Volume Flow cuft/hr 778.33 35264.27 2173790.00 61044.981992950.00 2524290.00 Enthalpy MMBtu/hr −8.07 0.02 −1077.90 −72.63−997.23 −1070.86 Mass Flow lb/hr N₂ 0.00 0.00 0.00 0.00 0.00 0.00 CO0.00 0.00 0.00 0.00 0.00 0.00 O₂ 0.00 19397.91 35012.55 0.00 15614.6435012.55 CO₂ 0.00 0.00 262947.01 0.00 262947.01 262947.01 DME 0.00 0.000.00 0.00 0.00 0.00 Isobutene 28291.20 0.00 28291.20 0.00 0.00 28291.20Acetaldehyde 0.00 0.00 0.00 0.00 0.00 0.00 Acrolein 0.00 0.00 0.00 0.000.00 0.00 Acetone 0.00 0.00 0.00 0.00 0.00 0.00 Methanol 0.00 0.00 0.000.00 0.00 0.00 MA 0.00 0.00 0.00 0.00 0.00 0.00 Water 0.00 0.00 15170.0812818.00 2352.08 15170.08 MMA 0.00 0.00 0.00 0.00 0.00 0.00 MNPK 0.000.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.00 0.00 0.00 0.00 0.00 Aceticacid 0.00 0.00 0.00 0.00 0.00 0.00 AA 0.00 0.00 0.00 0.00 0.00 0.00 MAA0.00 0.00 0.00 0.00 0.00 0.00 Heavy Ends 0.00 0.00 0.00 0.00 0.00 0.00H₂SO₄ 0.00 0.00 0.00 0.00 0.00 0.00 Heavy Organics 0.00 0.00 0.00 0.000.00 0.00 N-butane 0.00 0.00 0.00 0.00 0.00 0.00 Formaldehyde 0.00 0.000.01 0.00 0.01 0.01 Ethyl acetate 0.00 0.00 0.00 0.00 0.00 0.00 N-hexane0.00 0.00 0.00 0.00 0.00 0.00 Parameters S26 S28 S30 S32 S34 S36Temperature ° C. 390.00 29.44 71.06 364.94 225.00 280.00 (° F.) (734.00)(85.00) (159.90) (688.90) (437.00) (536.00) Pressure psi 22.00 100.0025.00 22.00 20.00 10.00 Vapor Frac 1.000 1.000 0.997 1.000 1.000 1.000Mole Flow lbmol/hr 8486.32 561.57 261.39 9309.27 9309.27 9259.68 MassFlow lb/hr 341420.85 17969.43 11939.87 371330.14 371330.14 371330.14Volume Flow cuft/hr 4937240.00 32667.37 68195.59 5210890.00 4470270.009886360.00 Enthalpy MMBtu/hr −1171.07 0.02 −31.31 −1202.36 −1229.59−1309.94 Mass Flow lb/hr N₂ 0.00 0.00 0.00 0.00 0.00 0.00 CO 1807.840.00 3.34 1811.18 1811.18 5161.99 O₂ 9089.28 17969.43 10.64 27069.3427069.34 11962.04 CO₂ 271490.60 0.00 5494.00 276984.60 276984.60283961.96 DME 0.00 0.00 0.00 0.00 0.00 0.00 Isobutene 452.66 0.00 0.00452.66 452.66 0.00 Acetaldehyde 488.69 0.00 117.99 606.68 606.68 121.34Acrolein 141.35 0.00 914.01 1055.36 1055.36 939.14 Acetone 527.15 0.001451.31 1978.45 1978.45 1582.76 Methanol 0.00 0.00 0.00 0.00 0.00 0.00MA 26683.31 0.00 2963.40 29646.71 29646.71 2994.32 Water 27033.62 0.00870.27 27903.89 27903.89 31606.88 MMA 0.00 0.00 0.00 0.00 0.00 0.00 MNPK0.00 0.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.00 0.00 0.00 0.00 0.00Acetic acid 1877.39 0.00 42.16 1919.55 1919.55 4612.02 AA 72.67 0.000.05 72.73 72.73 316.57 MAA 1345.70 0.00 72.70 1418.40 1418.40 27789.80Heavy ends 168.35 0.00 0.00 168.35 168.35 281.32 H₂SO₄ 0.00 0.00 0.000.00 0.00 0.00 Heavy organics 0.00 0.00 0.00 0.00 0.00 0.00 N-butane0.00 0.00 0.00 0.00 0.00 0.00 Formaldehyde 242.25 0.00 0.00 242.25242.25 0.00 Ethyl acetate 0.00 0.00 0.00 0.00 0.00 0.00 N-hexane 0.000.00 0.00 0.00 0.00 0.00

TABLE II Stream Properties in Quench Distillation Subsystem ParametersS38 S40 S42 S44 S46 S48 Temperature ° C. 67.00 66.94 66.94 67.00 66.9467.00 (° F.) (152.60) (152.50) (152.50) (152.60) (152.50) (152.60)Pressure psi 21.00 10.00 10.00 25.00 10.00 21.00 Vapor Frac 0.000 0.0000.000 0.000 0.000 0.000 Mole Flow lbmol/hr 62167.19 72057.12 71048.3271048.32 1008.80 71048.22 Mass Flow lb/hr 2501740.00 2899730.002859140.00 2859140.00 40596.27 2859140.00 Volume Flow cuft/hr 42208.4448921.52 48236.62 48237.79 684.90 48238.20 Enthalpy MMBtu/hr −8738.93−10129.33 −9987.52 −9987.36 −141.81 −9987.35 Mass Flow lb/hr N₂ 0.000.00 0.00 0.00 0.00 0.00 CO 0.70 0.81 0.80 0.80 0.01 0.80 O₂ 2.05 2.382.34 2.34 0.03 2.34 CO₂ 801.01 928.45 915.45 915.45 13.00 915.44 DME0.00 0.00 0.00 0.00 0.00 0.00 Isobutene 0.00 0.00 0.00 0.00 0.00 0.00Acetaldehyde 68.33 79.20 78.09 78.09 1.11 78.09 Acrolein 1008.16 1168.501152.14 1152.14 16.36 1152.18 Acetone 2575.57 2982.64 2940.88 2940.8841.76 2943.51 Methanol 0.00 0.00 0.00 0.00 0.00 0.00 MA 1886.65 2186.812156.20 2156.20 30.62 2156.18 Water 736412.06 853565.83 841615.91841615.91 11949.92 841613.78 MMA 0.00 0.00 0.00 0.00 0.00 0.00 MNPK 0.000.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.00 0.00 0.00 0.00 0.00 Aceticacid 162933.02 188853.63 186209.67 186209.67 2643.95 186209.17 AA19188.92 22241.59 21930.21 21930.21 311.38 21930.20 MAA 1559530.001807630.00 1782320.00 1782320.00 25306.81 1782320.00 Heavy Ends 17336.9420094.99 19813.66 19813.66 281.33 19813.65 H₂SO₄ 0.00 0.00 0.00 0.000.00 0.00 Heavy Organics 0.00 0.00 0.00 0.00 0.00 0.00 N-butane 0.000.00 0.00 0.00 0.00 0.00 Formaldehyde 0.00 0.00 0.00 0.00 0.00 0.00Ethyl acetate 0.00 0.00 0.00 0.00 0.00 0.00 N-hexane 0.00 0.00 0.00 0.000.00 0.00 Parameters S50 S52 S54 S56 S58 S60 Temperature ° C. 67.0048.78 55.06 55.06 55.06 60.72 (° F.) (152.60) (119.80) (131.10) (131.10)(131.10) (141.30) Pressure psi 21.00 20.00 20.00 20.00 20.00 8.00 VaporFrac 0.000 0.000 0.000 0.000 0.000 1.000 Mole Flow lbmol/hr 8881.0318732.26 27613.29 11830.98 15782.31 11200.73 Mass Flow lb/hr 357391.98635541.80 992933.78 425424.90 567508.87 398765.10 Volume Flow cuft/hr6029.78 10559.56 16586.05 7106.33 9479.72 8929850.00 Enthalpy MMBtu/hr−1248.42 −2554.80 −3803.22 −1629.50 −2173.72 −1549.04 Mass Flow lb/hr N₂0.00 0.00 0.00 0.00 0.00 0.00 CO 0.10 0.12 0.22 0.09 0.12 5161.97 O₂0.29 0.35 0.64 0.28 0.37 11961.98 CO₂ 114.43 170.06 284.49 121.89 162.60283956.42 DME 0.00 0.00 0.00 0.00 0.00 0.00 Isobutene 0.00 0.00 0.000.00 0.00 0.00 Acetaldehyde 9.76 15.63 25.39 10.88 14.51 121.34 Acrolein144.02 202.42 346.44 148.44 198.01 927.24 Acetone 367.94 730.34 1098.28470.56 627.72 1646.25 Methanol 0.00 0.00 0.00 0.00 0.00 0.00 MA 269.52383.42 652.94 279.75 373.19 2973.91 Water 105201.72 253366.76 358568.48153629.54 204938.94 68082.65 MMA 0.00 0.00 0.00 0.00 0.00 0.00 MNPK 0.000.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.00 0.00 0.00 0.00 0.00 Aceticacid 23276.15 46415.41 69691.56 29859.52 39832.04 8550.94 AA 2741.273857.98 6599.25 2827.47 3771.79 91.37 MAA 222790.06 327095.40 549885.46235599.77 314285.69 15291.03 Heavy Ends 2476.71 3303.94 5780.64 2476.733303.91 0.01 H₂SO₄ 0.00 0.00 0.00 0.00 0.00 0.00 Heavy Organics 0.000.00 0.00 0.00 0.00 0.00 N-butane 0.00 0.00 0.00 0.00 0.00 0.00Formaldehyde 0.00 0.00 0.00 0.00 0.00 0.00 Ethyl acetate 0.00 0.00 0.000.00 0.00 0.00 N-hexane 0.00 0.00 0.00 0.00 0.00 0.00 Parameters S62 S64S66 S68 S70 S72 Temperature ° C. 54.89 51.61 51.61 114.72 36.00 32.22 (°F.) (130.80) (124.90) (124.90) (238.50) (95.00) (90.00) Pressure psi6.00 5.00 5.00 10.00 6.00 5.00 Vapor Frac 0.418 1.000 0.000 1.000 0.7191.000 Mole Flow lbmol/hr 26983.04 11421.52 15561.52 11421.52 11421.528251.03 Mass Flow lb/hr 966273.97 403771.78 562502.19 403771.78403771.78 330739.43 Volume Flow cuft/hr 11785500.00 14176300.00 9358.758517360.00 8113200.00 9690730.00 Enthalpy MMBtu/hr −3722.76 −1575.49−2147.27 −1561.63 −1636.76 −1229.23 Mass Flow lb/hr N₂ 0.00 0.00 0.000.00 0.00 0.00 CO 5162.10 5162.00 0.09 5162.00 5162.00 5161.98 O₂11962.35 11962.07 0.28 11962.07 11962.07 11962.00 CO₂ 284119.01283989.85 129.16 283989.85 283989.85 283948.96 DME 0.00 0.00 0.00 0.000.00 0.00 Isobutene 0.00 0.00 0.00 0.00 0.00 0.00 Acetaldehyde 135.85123.80 12.05 123.80 123.80 120.23 Acrolein 1125.25 952.24 173.01 952.24952.24 922.84 Acetone 2273.96 1727.79 546.17 1727.79 1727.79 1544.47Methanol 0.00 0.00 0.00 0.00 0.00 0.00 Pressure psi 6.00 5.00 5.00 10.006.00 5.00 MA 3347.10 3026.54 320.56 3026.54 3026.54 2963.68 Water273021.58 71619.15 201402.44 71619.15 71619.15 19658.54 MMA 0.00 0.000.00 0.00 0.00 0.00 MNPK 0.00 0.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.000.00 0.00 0.00 0.00 Acetic acid 48382.98 9793.35 38589.62 9793.359793.35 1967.98 AA 3863.15 89.55 3773.60 89.55 89.55 5.20 MAA 329576.7115325.42 314251.29 15325.42 15325.42 2483.56 Heavy Ends 3303.92 0.003303.92 0.00 0.00 0.00 H₂SO₄ 0.00 0.00 0.00 0.00 0.00 0.00 HeavyOrganics 0.00 0.00 0.00 0.00 0.00 0.00 N-butane 0.00 0.00 0.00 0.00 0.000.00 Formaldehyde 0.00 0.00 0.00 0.00 0.00 0.00 Ethyl acetate 0.00 0.000.00 0.00 0.00 0.00 N-hexane 0.00 0.00 0.00 0.00 0.00 0.00 ParametersS74 S76 S78 S80 S82 Temperature ° C. 32.22 48.78 49.89 117.39 88.28 (°F.) (90.00) (119.80) (120.00) (243.30) (190.90) Pressure psi 5.00 5.0049.00 57.00 10.00 Vapor Frac 0.000 0.000 1.000 0.000 0.003 Mole Flowlbmol/hr 3170.49 18732.26 8251.03 1056.47 2065.27 Mass Flow lb/hr73032.34 635541.80 330739.43 22230.00 62826.27 Volume Flow cuft/hr1197.85 10559.31 1024360.00 401.47 5840.29 Enthalpy MMBtu/hr −407.53−2554.84 −1227.70 −130.65 −272.46 Mass Flow lb/hr N₂ 0.00 0.00 0.00 0.000.00 CO 0.02 0.12 5161.98 0.00 0.01 O₂ 0.07 0.35 11962.00 0.00 0.03 CO₂40.89 170.06 283948.96 0.00 13.00 DME 0.00 0.00 0.00 0.00 0.00 Isobutene0.00 0.00 0.00 0.00 0.00 Acetaldehyde 3.57 15.63 120.23 0.28 1.39Acrolein 29.40 202.42 922.84 0.85 17.21 Acetone 183.33 730.34 1544.4737.28 79.04 Methanol 0.00 0.00 0.00 0.00 0.00 MA 62.86 383.42 2963.680.00 30.62 Water 51960.60 253366.76 19658.54 17966.24 29916.16 MMA 0.000.00 0.00 0.00 0.00 MNPK 0.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.00 0.000.00 0.00 Acetic acid 7825.37 46415.41 1967.98 1873.72 4517.67 AA 84.353857.98 5.20 5.10 316.49 MAA 12841.86 327095.40 2483.56 2346.52 27653.33Heavy Ends 0.00 3303.94 0.00 0.00 281.33 H₂SO₄ 0.00 0.00 0.00 0.00 0.00Heavy Organics 0.00 0.00 0.00 0.00 0.00 N-butane 0.00 0.00 0.00 0.000.00 Formaldehyde 0.00 0.00 0.00 0.00 0.00 Ethyl acetate 0.00 0.00 0.000.00 0.00 N-hexane 0.00 0.00 0.00 0.00 0.00

TABLE III Stream Properties in Absorber/Stripper Subsystem ParametersS84 S86 S88 S96 S98 S100 Temperature ° C. 36.28 36.28 259.78 117.39117.39 117.39 (° F.) (97.30) (97.30) (499.60) (243.30) (243.30) (243.30)Pressure psi 48.00 53.00 34.00 27.00 27.00 57.00 Vapor Frac 0.000 0.0001.000 0.000 0.000 0.000 Mole Flow lbmol/hr 54439.25 54439.25 0.2454177.95 54177.95 54177.95 Mass Flow lb/hr 1151940.00 1151940.00 10.001140000.00 1140000.00 1140000.00 Volume Flow cuft/hr 18937.37 18937.4570.95 20587.33 20587.33 20588.25 Enthalpy MMBtu/hr −6879.53 −6879.51−0.04 −6699.93 −6699.93 −6699.79 Mass Flow lb/hr N₂ 0.00 0.00 0.00 0.000.00 0.00 CO 3.34 3.34 0.00 0.00 0.00 0.00 O₂ 10.08 10.08 0.56 0.00 0.000.00 CO₂ 5484.75 5484.75 9.36 0.03 0.03 0.03 DME 0.00 0.00 0.00 0.000.00 0.00 Isobutene 0.00 0.00 0.00 0.00 0.00 0.00 Acetaldehyde 132.29132.29 0.00 14.27 14.27 14.27 Acrolein 957.90 957.90 0.00 43.79 43.7943.79 Acetone 3366.66 3366.66 0.00 1911.95 1911.95 1911.95 Methanol 0.000.00 0.00 0.00 0.00 0.00 MA 2963.68 2963.68 0.00 0.00 0.00 0.00 Water922217.22 922217.22 0.08 921345.66 921345.66 921345.66 MMA 0.00 0.000.00 0.00 0.00 0.00 MNPK 0.00 0.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.000.00 0.00 0.00 0.00 Acetic acid 96130.36 96130.36 0.00 96088.13 96088.1396088.13 AA 261.75 261.75 0.00 261.70 261.70 261.70 MAA 120407.30120407.30 0.00 120334.47 120334.47 120334.47 Heavy Ends 0.00 0.00 0.000.00 0.00 0.00 H₂SO₄ 0.00 0.00 0.00 0.00 0.00 0.00 Heavy Organics 0.000.00 0.00 0.00 0.00 0.00 N-butane 0.00 0.00 0.00 0.00 0.00 0.00Formaldehyde 0.00 0.00 0.00 0.00 0.00 0.00 Ethyl acetate 0.00 0.00 0.000.00 0.00 0.00 N-hexane 0.00 0.00 0.00 0.00 0.00 0.00 Parameters S102S104 S106 S108 S110 S112 Temperature ° C. 117.39 21.11 21.11 21.1 15.5617.22 (° F.) (243.30) (70.00) (70.00) (70.00) (60.00) (63.00) Pressurepsi 57.00 49.00 49.00 49.00 47.00 43.00 Vapor Frac 0.000 0.000 0.0000.000 0.000 1.000 Mole Flow lbmol/hr 53121.48 53121.52 45153.29 7968.237968.23 6930.93 Mass Flow lb/hr 1117770.00 1117770.00 950104.50167665.50 167665.50 296470.63 Volume Flow cuft/hr 20186.78 18088.3215375.07 2713.25 2698.10 887191.07 Enthalpy MMBtu/hr −6569.14 −6736.03−5725.63 −1010.40 −1011.75 −1085.15 Mass Flow lb/hr N₂ 0.00 0.00 0.000.00 0.00 0.00 CO 0.00 0.00 0.00 0.00 0.00 5159.53 O₂ 0.00 0.00 0.000.00 0.00 11949.69 CO₂ 0.03 0.03 0.02 0.00 0.00 278362.13 DME 0.00 0.000.00 0.00 0.00 0.00 Isobutene 0.00 0.00 0.00 0.00 0.00 0.00 Acetaldehyde13.99 13.98 11.89 2.10 2.10 1.93 Acrolein 42.93 42.91 36.47 6.44 6.447.91 Acetone 1874.67 1873.32 1592.32 281.00 281.00 51.40 Methanol 0.000.00 0.00 0.00 0.00 0.00 MA 0.00 0.00 0.00 0.00 0.00 0.00 Water903379.42 903380.52 767873.45 135507.08 135507.08 821.55 MMA 0.00 0.000.00 0.00 0.00 0.00 MNPK 0.00 0.00 0.00 0.00 0.00 0.00 Toluene 0.00 0.000.00 0.00 0.00 0.00 Acetic acid 94214.41 94214.52 80082.34 14132.1814132.18 52.11 AA 256.60 256.60 218.11 38.49 38.49 0.05 MAA 117987.95117988.12 100289.90 17698.22 17698.22 64.34 Heavy Ends 0.00 0.00 0.000.00 0.00 0.00 H₂SO₄ 0.00 0.00 0.00 0.00 0.00 0.00 Heavy Organics 0.000.00 0.00 0.00 0.00 0.00 N-butane 0.00 0.00 0.00 0.00 0.00 0.00Formaldehyde 0.00 0.00 0.00 0.00 0.00 0.00 Ethyl acetate 0.00 0.00 0.000.00 0.00 0.00 N-hexane 0.00 0.00 0.00 0.00 0.00 0.00

TABLE IV Stream Properties in Stripper Gas Subsystem Parameters S114S115 S116 S118 S120 S122 Temperature ° C. 141.61 161.89 20 364.94 260259.78 (° F.) (286.90) (323.40) (68.00) (688.90) (500.00) (499.60)Pressure psi 45.00 45.00 43.00 38.00 34.00 34.00 Vapor Frac 1.000 0.4080.998 1.000 1.000 1.000 Mole Flow lbmol/hr 10.17 11.49 6952.59 7289.347289.34 695.83 Mass Flow lb/hr 533.14 1066.72 298070.50 310570.50310570.50 29646.76 Volume Flow cuft/hr 1758.30 821.48 897045.562362510.00 2202390.00 210329.19 Enthalpy MMBtu/hr −0.76 −1.55 −1087.46−1087.48 −1102.51 −105.24 Mass Flow lb/hr N₂ 0.00 0.00 0.00 0.00 0.000.00 CO 0.01 0.00 5159.54 0.00 0.00 0.00 O₂ 0.03 0.00 11949.72 17263.1117263.11 1647.92 CO₂ 13.00 0.00 278375.13 290706.98 290706.98 27750.61DME 157.70 0.00 157.70 0.00 0.00 0.00 Isobutene 0.00 0.00 0.00 0.00 0.000.00 Acetaldehyde 1.37 0.02 3.32 0.00 0.00 0.00 Acrolein 16.99 0.1525.05 0.00 0.00 0.00 Acetone 74.16 1.60 127.16 0.00 0.00 0.00 Methanol28.20 0.00 28.20 0.00 0.00 0.00 MA 30.43 0.15 30.58 0.00 0.00 0.00 Water24.20 3.61 849.36 2600.39 2600.39 248.23 MMA 0.06 0.00 0.06 0.00 0.000.00 MNPK 0.00 0.00 0.00 0.00 0.00 0.00 Toluene 83.08 0.02 83.10 0.000.00 0.00 Acetic acid 13.98 29.00 95.08 0.00 0.00 0.00 AA 0.00 288.89288.93 0.00 0.00 0.00 MAA 0.02 45.07 109.43 0.00 0.00 0.00 Heavy Ends0.00 281.35 281.35 0.00 0.00 0.00 H₂SO₄ 0.00 0.00 0.00 0.00 0.00 0.00Heavy Organics 0.00 0.00 0.00 0.00 0.00 0.00 N-butane 0.00 0.00 0.000.00 0.00 0.00 Formaldehyde 0.00 0.01 0.01 0.01 0.01 0.00 Ethyl acetate6.32 4.30 10.61 0.00 0.00 0.00 N-hexane 83.60 412.56 496.15 0.00 0.000.00

The overall separation efficiencies of the columns utilized in thissystem are tabulated in Table V.

TABLE V Separation Efficiencies Product Losses as Percentage of TotalProduct Made Separation Unit Product Loss Quench Column 0.14 AbsorberColumn 0.23 Stripper Column 0.05 Overall 0.42

All references cited herein are incorporated by reference. While thisinvention has been described fully and completely, it should beunderstood that, within the scope of the appended claims, the inventionmay be practiced otherwise than as specifically described. Although theinvention has been disclosed with reference to its preferredembodiments, from reading this description those of skill in the art mayappreciate changes and modification that may be made which do not departfrom the scope and spirit of the invention as described above andclaimed hereafter.

We claim:
 1. (canceled)
 2. (canceled)
 3. (canceled)
 4. A quench columnapparatus comprising: a quench column including a feed port forintroducing a hot stream comprising methacrolein (MA), methacrylic acid(MAA) and acetic acid (AA) into the quench column, where the feed portis located above a liquid level in the quench column, a bottom port forwithdrawing a bottoms stream from the quench column, a top port forwithdrawing an overhead stream from the quench column, a quench port forintroducing a quench stream into the quench column, where the quenchport is located above the feed port, and an upper port for introducing aliquid stream comprising overhead condensibles and a second portion ofthe bottoms stream to improve liquid-gas interactions within the quenchcolumn, a bottoms recycle system including: a first splitter valve todivide the bottoms stream into a product stream and a recycle stream,and a second splitter valve to divide the recycle stream into the quenchstream and a top recycle stream, a top recycle system including: atleast one separator to separate the overhead stream into a vapor streamand an overhead liquid stream, and a mixing valve to combine the liquidstream and the top recycle stream forming the liquid stream, where: amass ratio of the first portion of the bottoms stream to the hot streamis set to rapidly reduce a temperature of the hot oxidized stream to atemperature at or below about 75° C., and a mass ratio of the firstportion of the bottoms stream to the second portion of the bottomsstream is at least 5:1, and.
 5. The apparatus of 4, wherein the firstmass ratio is at least 6:1, the second mass ratio is about 5.5:1 and thetemperature at or below about 70° C.
 6. The apparatus of 4, wherein thefirst mass ratio is at least 7:1, the second mass ratio is about 6:1 andthe temperature at or below about 67° C.
 7. (canceled)
 8. (canceled) 9.(canceled)
 10. (canceled)
 11. (canceled)
 12. (canceled)
 13. (canceled)14. (canceled)
 15. (canceled)
 16. (canceled)
 17. (canceled) 18.(canceled)
 19. (canceled)
 20. (canceled)
 21. (canceled)
 22. (canceled)23. (canceled)
 24. (canceled)
 25. (canceled)
 26. (canceled) 27.(canceled)
 28. (canceled)
 29. The apparatus of 4, wherein the first massratio is at least 5:1 and the second mass ratio is about 5:1.
 30. Theapparatus of 4, wherein the first mass ratio is at least 5:1.
 31. Theapparatus of 4, wherein the first mass ratio is at least 6:1.
 32. Theapparatus of 4, wherein the first mass ratio is at least 7:1.
 33. Theapparatus of 4, wherein the second mass ratio is about 5.5:1.
 34. Theapparatus of 4, wherein the second mass ratio is about 6:1.
 35. Theapparatus of 4, wherein the temperature is at or below about 70° C. 36.The apparatus of 4, wherein the temperature is at or below about 67° C.